About this trial
This is a prospective, parallel, non-blinded, two-arm randomized controlled trial of intravenous catheter failure evaluating the impact of a built-in guide wire. The objective of this study is to demonstrate that the control ultralong intravenous catheter (IV) without the guide wire is non-inferior to the experimental catheter with the guide wire. After obtaining consent, eligible patients will be randomly allocated to control Arm 1 (ultralong intravenous catheter) or experimental Arm 2 (ultralong intravenous catheter with guide wire) in a ratio of 1:1 via a computer-generated randomization schedule. The participants will be followed to collect data until the catheter is removed.
Eligibility criteria
Qualifiers
Visible with distention and easily palpable
Visible and easily palpable
Not visible and easily palpable
Visible and poorly palpable
Disqualifiers
None
Trial design
Treatments tested in this trial
- B. Braun 6.35cm 20 gauge ultralong intravenous catheter
- BD 5.71 cm 20 gauge Accucath